A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12897855



Internal ID827550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94818052..94827480hg38UCSC Ensembl
Innerchr7:94818088..94827445hg38UCSC Ensembl
Outerchr7:94818017..94827516hg38UCSC Ensembl
chr7:94447364..94456792hg19UCSC Ensembl
Innerchr7:94447400..94456757hg19UCSC Ensembl
Outerchr7:94447329..94456828hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg389429
hg199429
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614185
Supporting Variants
SamplesHG00410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12897855
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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